Canonical Allele Identifier: CA1474562158
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007786_88007787delinsCG , CM000666.2:g.88007786_88007787delinsCG GRCh38
NC_000004.11:g.88928938_88928939delinsCG , CM000666.1:g.88928938_88928939delinsCG GRCh37
NC_000004.10:g.89147962_89147963delinsCG NCBI36
NG_008604.1:g.5119_5120delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.53_54delinsCG MANE Select ENSP00000237596.2:p.Pro18=
ENST00000237596.6:c.53_54delinsCG ENSP00000237596.2:p.Pro18=
NM_000297.3:c.53_54delinsCG NP_000288.1:p.Pro18=
XM_011532028.1:c.53_54delinsCG XP_011530330.1:p.Pro18=
XR_244632.2:n.148_149delinsCG
NR_156488.1:n.140_141delinsCG
XM_011532028.2:c.53_54delinsCG XP_011530330.1:p.Pro18=
NM_000297.4:c.53_54delinsCG MANE Select NP_000288.1:p.Pro18=
NR_156488.2:n.152_153delinsCG